Graft copolymers and method to prepare same

ABSTRACT

A thermally processable graft copolymer formed from a water soluble polymer and a water insoluble polymer, wherein the graft copolymer forms a hydrogel upon exposure to water. A method to form such a hydrogel-forming graft copolymer by copolymerizing a water soluble 2-substituted-2-oxazolines with a water insoluble 2-substituted-2-oxazoline. A method to form such a hydrogel-forming graft copolymer by transamidating a poly-2-oxazoline with a carboxylic acid terminated water-insoluble polymer.

FIELD OF THE INVENTION

[0001] Applicants' invention comprises polyoxazoline-based thermoplastic, polymeric hydrogel compositions that can be formed into useful articles by conventional molding processes, such as injection molding, compression molding, and extrusion, wherein those molded articles have the properties of a hydrogel material. Applicants' invention further comprises two methods for forming these novel thermoplastic, polymeric hydrogel compositions.

BACKGROUND OF THE INVENTION

[0002] Hydrogel-forming polymers are those which are not water soluble, but which upon contacting aqueous fluids, imbibe such fluids. Upon absorbing water, the mechanical properties of articles formed from such polymeric hydrogel materials change. For example, articles which are rigid when dry may become soft and pliable when wet.

[0003] Certain of these systems are used in commerce ranging from use as “supersorbers” in baby diapers to more sophisticated uses in the manufacture of soft contact lenses. Polymer hydrogel systems include ionically linked hydrogels, covalently crosslinked hydrogels, and the like.

[0004] Ionic hydrogels are polymers containing functional groups that ionically bond to form a crosslinked system. Such materials are used to form toy products that can be continuously reformed and reshaped. These materials, however, cannot be formed into a permanent shape or configuration.

[0005] Covalently crosslinked hydrogels are formed by crosslinking otherwise water-soluble polymers. Once these materials are crosslinked, they will no longer dissolve in water, or in any other solvent for that matter. Nevertheless, these crosslinked materials will absorb water and swell in dimension. Compositions such as crosslinked poly-2-hydroxyethylmethacrylate are used to form contact lenses. These materials, however, cannot be thermally processed.

[0006] Mechanically crosslinked systems are formed when two polymers which are incompatible are chemically linked as either block copolymers or graft copolymers. On the one hand, if the two incompatible homopolymers are simply blended together, a gross phase separation occurs. If on the other hand, the two polymers or connected together covalently, a microphase separation occurs.

[0007] This microphase separation is a well known phenomenon that has been utilized, most notably, in the styrene-butadiene Kraton triblock rubber field. Block copolymers partition into different phases, a continuous phase consisting of the higher percentage polymer and a discontinuous or dispersed phase consisting of the lower percentage polymer. The dispersed phase can form very distinct domains, including spheres, cylinders, and lamella. The configuration of these domains is related to the relative percentages of the two phases. At low percentages, the dispersed phase comprises spherical domains. As that percentage increases the dispersed phase forms cylindrical domains and finally discrete lamella.

[0008] Significantly, a microphase separated two-component polymeric material exhibits two glass transition temperatures (t_(g)'s), namely one for each polymer present. When the temperature of the composite material is below the respective glass transition temperatures of both components, the copolymer is rigid. If the composite material is warmed above the glass transition temperatures of both phases, the copolymer will flow. Therefore, such a mechanically crosslinked copolymer can be thermally processed using conventional molding techniques such as extrusion and injection molding.

[0009] A mechanically crosslinked hydrogel copolymer comprises a block or graft copolymer formed from incompatible polymers where the continuous phase is a water soluble polymer. Various water soluble organic polymers prepared from substituted ethylenes are known, including polyvinylpyrrolidone, polyvinylalcohol, and the like. Polyethylenimine, and certain of its derivatives is also water soluble.

[0010] Poly-2-alkyl-2-oxazolines, where the alkyl group comprises 1-5 carbons, are such water soluble, N-acyl polyethyleneimines. Significantly, these poly-2-alkyl-2-oxazolines have thermal properties that differ materially from water soluble polymers prepared from substituted ethylenes. For example, poly-2-ethyl-2-oxazoline has both a low dry glass transition temperature of 70-71° C. and a high thermal degradation temperature above 380° C.

[0011] Prior art mechanically crosslinked hydrogel systems do not include systems based upon poly-2-alkyl-2-oxazolines. U.S. Pat. No. 4,582,877, in the name of Fairchok et al., teaches a method to enhance the wettability of polypropylene by blending polypropylene with substituted polyethyleneimines. Fairchok et al. teaches preparation of those substituted polyethyleneimines by reacting a poly-2-oxazoline with a carboxylic acid to form a polyethyleneimine having pendent groups of up to 22 carbon atoms. Col. 1/1. 50 to Col. 2/1. 17. Each such 22 carbon pendent side group would increase the molecular weight of the polyethyleneimine by only about 300 grams/mole. In a most preferred embodiment, Fairchok et al. teaches preparation of a covalently crosslinked material by reacting a poly-2-oxazoline with a polybasic carboxylic acid. Col. 2/1. 18-25.

[0012] In contrast, Applicant's invention comprises a graft copolymer comprising a water soluble poly-2-alkyl-oxazoline having a plurality of pendent non-water soluble polymers grafted thereon, wherein each of the pendent non-water soluble polymers has a number average molecular weight of at least 5,000. Moreover, Applicants' invention does not encompass any covalently crosslinked systems.

SUMMARY OF THE INVENTION

[0013] In a first embodiment, Applicants' novel invention comprises a thermally processable graft copolymer formed from a water soluble polymer and a water insoluble polymer, wherein that graft copolymer forms a hydrogel upon exposure to water. The water soluble portion of Applicants' novel graft copolymer is formed from a poly-2-substituted-2-oxazoline. The water insoluble portion of the graft copolymer is formed from a polyalkyleneoxide polymer/copolymer, long chain alkyl, polybutadiene, polyisoprene, a polyester, a polyamide, or a polyurethane.

[0014] A second embodiment of the instant invention comprises a novel method to form such a hydrogel forming graft copolymer by copolymerizing a first 2-substituted-2-oxazolines with a second 2-substituted-2-oxazoline. Such a copolymerization can be performed neat or in solution.

[0015] A third embodiment of Applicants' invention comprises a novel method to form such a hydrogel-forming graft copolymer by transamidating a poly-2-oxazoline with a carboxylic acid terminated water-insoluble polymer. In the alternative, an amide exchange reaction is performed using a polymeric acid chloride, a polymeric acid salt, or a polymeric anhydride.

BRIEF DESCRIPTION OF THE DRAWINGS

[0016] The invention will be better understood from a reading of the following detailed description taken in conjunction with the drawings in which like reference designators are used to designate like elements, and in which:

[0017]FIG. 1 is a perspective view depicting the structure of Applicants' novel graft copolymer according to the present invention; and

[0018]FIG. 2 is a perspective view depicting the configuration of Applicants' novel graft copolymer in an aqueous environment.

DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS

[0019] Referring to FIG. 1, applicants' invention is shown as graft copolymer system 10, which comprises a water soluble polymer 12 having one or more pendent non-water soluble polymers 14 and 16 grafted thereon. Although FIG. 1 depicts two non-water soluble polymers, i.e. polymer 14 and polymer 16, grafted onto water soluble polymer 12, Applicants' invention includes graft copolymers in which a plurality of non-water soluble polymers are grafted onto a water soluble polymer backbone.

[0020] Turning to FIG. 2, the configuration of three different copolymer chains in an aqueous environment is shown. The water soluble portions of these copolymers, i.e. 12(a), 12(b), and 12(c), remain individually dispersed in the solvent. The water insoluble portions, however, aggregate to form discrete domains 18(a), 18(b), and 18(c). These dispersed domains function as “mechanical” crosslinks thereby giving copolymer 12 certain physical properties generally found only in covalently crosslinked polymers. Copolymer 12, however, contains no actual covalent crosslinks, and therefore, is thermally processable.

[0021] Water soluble portion 12 of graft copolymer 12 comprises a substituted poly-N-acyl-ethyleneimine having structure I

[0022] wherein R₁ is a hydrogen or an alkyl group having 1 to 4 carbons. Polymer I has a number average molecular weight of between about 5,000 to about 1,000,000, preferably between about 10,000 to about 100,000, and most preferably between about 25,000, and about 75,000. Substituted polyethyleneimine I is prepared by a cationic ring opening polymerization of 2-R₁-2-

[0023] oxazoline III using catalyst IV, where R′ is hydrogen, alkyl, aralkyl, and mixtures thereof, and X is acetate, p-tosylate, halide, sulfate, triflate, and mixtures thereof. For example, methyl triflate can be used as initiator IV, in which case R′ is methyl and X is triflate. The cationic ring opening polymerization of monomer III can be conducted neat or in solvent. Solvents for this ring opening polymerization include orthodichlorobenzene, ethyl benzene, cumene, xylene, decane, 2-ethyl hexyl acetate, naphthalene, and octane. For example, the polymerization can be carried out in orthodichlorobenzene at a temperature between about 7° C. and about 180° C.

[0024] In a most preferred embodiment, R, is ethyl, and polymer I has a number average molecular weight of about 50,000. This poly-2-ethyl-2-oxazoline polymer is sold commercially under the name of AQUASOL 50 by Polymer Chemistry Innovations, Inc., the assignee of this application.

[0025] To form the mechanically crosslinkable polymeric hydrogel of the present invention, up to about 20% of the pendent R₁ groups on polymer I are replaced by a water soluble polymer to form a graft copolymer of structure II

[0026] The WATER INSOLUBLE POLYMER portion of graft copolymer II is a non-water soluble polymeric material having a number average molecular weight between about 5,000 and 100,000, preferably between about 8,000 and about 20,000, and most preferably between about 10,000 and 15,000. The WATER INSOLUBLE POLYMER includes polyethylene, long chain alkyl, polypropylene, polybutadiene, polyisoprene, polystyrene, polymethylacrylate, polymethylmethacrylate, polyurethanes, polyamides, polyesters, polyesteramides, and copolymers of same.

[0027] In a first embodiment, graft copolymer II is formed by a transamidation reaction. In general, transamidation is accomplished by reacting an amide of one carboxylic acid with a second carboxylic acid. A mixture of amides usually results. For example, if amide V is reacted with carboxylic acid VI, transamidation occurs to yield a mixture of amides V and VII.

[0028] If carboxylic acid VII is removed from the reaction as it forms, however, the equilibrium will be continuously shifted to produce more amide VII. Therefore, amide V can be essentially completely converted to amide VII if acid VIII is removed as it forms.

[0029] A similar amide exchange reaction can also be performed by reacting an amide of a first carboxylic acid with a second acid salt, a second acid chloride, and/or a second acid anhydride. The transamidation reactions discussed below used to prepare graft copolymers can also use a polymeric acid salt, a polymeric acid chloride, and/or a polymeric acid anhydride.

[0030] Graft copolymer II, where the WATER INSOLUBLE PORTION comprises polystyrene, polybutadiene, polyisoprene, polymethylacrylate, polymethylmethacrylate, or copolymers of

[0031] same, is formed by reacting polymer I with a carboxylic acid terminated polymer having structure IX. Polymer IX can be prepared by an anionically catalyzed polymerization. For example, where R₂ is phenyl, ethylenyl, isopropenyl, or carbomethoxy, and R₃ is either hydrogen or methyl, water-insoluble polymer XI can be formed by an anionic polymerization of monomer X to yield lithium-terminated living polymer XI which is reacted with carbon dioxide to give lithium carboxylate terminated polymer XII.

[0032] Reaction of one mole of polymer I where R₁ is ethyl with 0.20 moles of acid terminated polymer XII where R₂ is phenyl and R₃ is hydrogen, along with removal of the proprionic acid formed, will yield a graft copolymer having the structure XIII. Preferably, the number average

[0033] molecular weight of graft copolymer XIII is between about 1,000 and about 10,000,000 with m being between about 1 and about 10,000

[0034] Alternatively, the WATER INSOLUBLE PORTION of graft copolymer H can comprise a polyethyleneoxide, a polypropyleneoxide, or a polyethyleneoxide-co-polypropylene oxide. Such a graft copolymer is prepared by a transamidation reaction of polymer I with a carboxylic acid terminated polyalkyleneoxide polymer or copolymer.

[0035] A carboxylic acid terminated polyethylene oxide polymer can be prepared by anionic ring opening polymerization of ethylene oxide XIV to give lithium-terminated polyethylene oxide XV (R₁₀ is hydrogen). Lithium-terminated polyethyleneoxide XV is reacted with acrylic acid and then quenched to give acid terminated polyethylene oxide XVI.

[0036] Graft copolymer II can be formed by partial transamidation of polymer I with polymer XVI. As an example, 0.20 moles of carboxylic acid terminated polyethyleneoxide XVI (R₁₀═H) are reacted with 1.0 moles of polymer I (R1=ethyl), with removal of the proprionic acid as it forms, to prepare graft copolymer XVII.

[0037] The WATER INSOLUBLE PORTION of graft copolymer II prepared by transamidation can also comprise a polyester or a polyamide. Carboxylic acid terminated polyester XXI can be prepared by reacting between about 0.1 to about 0.2 equivalents of monofunctional alcohol XVIII, 1.0 equivalents of diacid XIX, and between about 0.8 to about 0.9 equivalents of diol XX. Preferably diacid XIX comprises adipic acid, i.e. q is 4, and diol XX comprises hexahediol, i.e. r is 6.

[0038] Graft copolymer II, where the WATER INSOLUBLE POLYMER comprises a polyester can be prepared by partial transamidation of polymer I with carboxylic acid terminated polyester XXI to give a graft copolymer having a number average molecular weight of between about 1,000 and about 10,000,000 with s being between about 2 and about 1,000,000.

[0039] In a second embodiment, graft copolymer II can be prepared by copolymerization rather than by transamidation. For example, monomer III and monomer XXII can be copolymerized to form graft copolymer II.

[0040] As in the transamidation embodiment discussed above, the WATER INSOLUBLE POLYMER portion of monomer XXII is selected from the group consisting of polyesters, polyamides, polyesteramides, polyurethanes, polyethyleneoxide, polypropyleneoxide, polyethyleneoxide-co-polypropyleneoxide, polybutadiene, polyisoprene, polymethylacrylate, polymethylmethacrylate, polystyrene, and copolymers of same.

[0041] Where the WATER INSOLUBLE POLYMER portion comprises polybutadiene, polyisoprene, polymethylacrylate, polymethylmethacrylate, or polystyrene, monomer XXII can be prepared by using the lithium salt of 2-methyl-2-oxazoline as an anionic polymerization initiator.

[0042] Lithium diisopropylamide XXIII can be prepared by adding a 1.5 M solution of n-BuLi in THF to diisopropylamine in THF at 0° C. After about 30 minutes that solution can be cooled to −78° C. and transferred via cannula to a precooled solution of 2-methyl-2-oxazoline in THF at −78° C. to form initiator XXIV. Initiator XXIV is added to an excess of anionically-polymerizable monomer to form a lithium-terminated polymer which after quenching with an acid yields 2-substituted-2-oxazoline XXV.

[0043] Copolymerization of 1.0 moles of monomer III where R₁ is ethyl with 0.20 moles of monomer XXV where R₂ is hydrogen and R₃ is phenyl yields graft copolymer XIII. This copolymerization can be performed neat or in solvent.

[0044] As those skilled in the art will appreciate, a carboxylic acid terminated polyamide can be similarly formed from a condensation reaction of about 0.1 to about 0.2 equivalents of a monoamine, 1.0 equivalents of a diacid, and about 0.8 to about 0.9 equivalents of a diamine, with continuous removal of the water formed. Moreover, reaction of about 0.1 equivalents of a monoamine, 1.0 equivalents of a diacid, and about 0.8 to about 0.9 equivalents of a mixture of a diol and diamine, will form a carboxylic acid terminated polyesteramide.

[0045] In order to prepare graft copolymer II where the WATER INSOLUBLE POLYMER comprises a polyalkyleneoxide polymer or copolymer, initiator XXI can be used to anionically polymerize ethylene oxide (XIV with R₁₀═H) and/or propylene oxide (XIV with R₁₀=methyl) to form 2-polyethylene oxide-2-oxazoline XXIX (R₁₀═H), 2-polypropylene oxide-2-oxazoline XXIX (R₁₀=methyl), or 2-polyethyleneoxide-co-polypropyleneoxide-2-oxazoline XXX. As those skilled in the art will appreciate, 2-oxazoline-terminated copolymer XXX may comprise a random copolymer of ethylene oxide units and propylene oxide units, or a block copolymer of alternating ethylene oxide blocks and propylene oxide blocks.

[0046] Monomer XXIX can be copolymerized with monomer III to form graft copolymer II. The cationic ring-opening copolymerization can be carried out neat or in solvent. For example, copolymerizing 1.0 moles of monomer III, where R₁ is ethyl, with 0.20 moles of monomer XXIX, where R₁₀ is hydrogen, forms graft copolymer XXXI.

[0047] Alternatively, copolymerization of monomer XXXIII with monomer III gives a graft copolymer where the WATER INSOLUBLE POLYMER portion comprises a polyester. Carboxylic acid terminated polyester XXI is reacted with ethanolamine to form beta-, hydroxyamide terminated polyester XXXII which is subsequently cyclized with removal of one mole of water to form monomer XXXIII.

[0048] Preferably, the graft copolymer formed by the cationic ring-opening copolymerizing monomer III where R₁ is ethyl, and monomer XXXIII, where q is 4 and r is 6, has a number average molecular weight between about 100 and about 10,000,000 with s being between about 2 and about 1,000,000.

[0049] While the preferred embodiments of the present invention have been illustrated in detail, it should be apparent that modifications and adaptations to those embodiments may occur to one skilled in the art without departing from the scope of the present invention as set forth in the following claims. 

We claim:
 1. A polymeric material having the structure

wherein R₁ is selected from the group consisting of hydrogen, methyl, ethyl, and propyl, X is selected from the group consisting of acetate, p-tosylate, halide, sulfate, triflate, and mixtures thereof, and POLYMER2 is a water-insoluble polymeric material having a number average molecular weight in excess of 5,000.
 2. The composition of claim 1, wherein POLYMER2 has the structure

wherein R₂ is selected from the group consisting of hydrogen, methyl, and mixtures thereof, and R₃ is selected from the group consisting of hydrogen, methyl, ethenyl, isopropenyl, carbomethoxy, phenyl, and mixtures thereof.
 3. The composition of claim 2, wherein n is between about 50 to about 10,000, m is adjusted such that m/(n+m) is between about 0.0001 to about 0.20, and p is between about 60 to about
 1250. 4. The composition of claim 1, wherein POLYMER2 has the structure

wherein R₄ is selected from the group consisting of hydrogen, methyl, and mixtures thereof, and R₅ is hydrogen or alkyl.
 5. The composition of claim 4, wherein n is between about 50 to about 10,000, m is adjusted such that m/(n+m) is between about 0.0001 to about 0.20, p is between about 60 to about
 1250. 6. The composition of claim 1, wherein POLYMER 2 has the structure

wherein Z is selected from the group consisting of O, NH, and mixtures thereof, and R₆ is selected from the group consisting of methyl, ethyl, propyl, and butyl.
 7. The composition of claim 6, wherein n is between about 50 to about 10,000, m is adjusted such that m/(n+m) is between about 0.0001 to about 0.20, q is between 4 to about 12, r is between 4 to about 12, s is between about 25 to about 450
 8. A method to form a polymeric composition having the structure

wherein R₁ is selected from the group consisting of hydrogen, methyl, ethyl, and propyl, X is selected from the group consisting of acetate, p-tosylate, halide, sulfate, triflate, and mixtures thereof, and POLYMER2 is a non-water soluble polymeric material having a number average molecular weight of 5,000 or greater; comprising the steps of: supplying a first monomer having the structure

 wherein R1 is selected from the group consisting of hydrogen, methyl, ethyl, and propyl; supplying a second monomer having the structure

 wherein POLYMER2 is a non-water soluble polymeric material having a number average molecular weight of 5,000 or greater; mixing said second monomer with said first monomer; adding a cationic polymerization catalyst R′X to said monomer mixture to form a reaction mixture, wherein X is selected from the group consisting of acetate, p-tosylate, halide, sulfate, triflate, and mixtures thereof, and wherein R′ is selected from the group consisting of hydrogen, alkyl, or aralkyl; stirring said reaction mixture; and heating said reaction mixture at a temperature of between about 7° C. to about 180° C. to form said polymeric composition.
 9. The method of claim 8, wherein said heating step is performed in a solvent.
 10. The method of claim 9, wherein said solvent is selected from the group consisting of orthodichlorobenzene, ethyl benzene, cumene, xylene, decane, 2-ethyl hexyl acetate, naphthalene, octane, and mixtures thereof.
 11. The method of claim 8, wherein POLYMER2 has the structure

wherein R₂ is selected from the group consisting of hydrogen, methyl, and mixtures thereof, and R₃ is selected from the group consisting of hydrogen, methyl, carbomethoxy, ethenyl, isopropenyl, phenyl, and mixtures thereof.
 12. The method of claim 11, wherein n is between about 50 to about 10,000, m is adjusted such that m/(n+m) is between about 0.0001 to about 0.20, and p is between about 60 to about
 1250. 13. The method of claim 8, wherein POLYMER2 has the structure

wherein R₇ is selected from the group consisting of hydrogen, methyl, and mixtures thereof
 14. The method of claim 13, wherein n is between about 50 to about 10,000, m is adjusted such that m/(n+m) is between about 0.0001 to about 0.20, 1 is between about 60 to about
 1250. 15. The method of claim 8, wherein POLYMER2 has the structure

wherein Z is selected from the group consisting of O, NH, and mixtures thereof, and R₈ is selected from the group consisting of methyl, ethyl, propyl, and butyl.
 16. The method of claim 15, wherein n is between about 50 to about 10,000, m is adjusted such that m/(n+m) is between about 0.0001 to about 0.20, q is between 4 to about 12, r is between 4 to about 12, s is between about 25 to about
 450. 17. A method to form a polymeric composition having the structure

wherein R₁ is selected from the group consisting of hydrogen, methyl, ethyl, and propyl, X is selected from the group consisting of acetate, p-tosylate, halide, sulfate, triflate, and mixtures thereof, and POLYMER2 is a water-insoluble polymeric material having a number average molecular weight of 5,000 or greater; comprising the steps of: supplying a first polymer having the structure

 wherein R₁ is selected from the group consisting of hydrogen, methyl, ethyl, and propyl, and X is selected from the group consisting of acetate, p-tosylate, halide, sulfate, triflate, and mixtures thereof; supplying a second polymer having the structure

 wherein POLYMER2 is a non water soluble polymeric material having a number average molecular weight of 5,000 or greater, and Y is selected from the group consisting of OH, Cl, O⁻Na⁺, O⁻K⁺, and O⁻Li⁺; mixing said second polymer with said first polymer to form a reaction mixture; stirring said reaction mixture; and heating said reaction mixture while removing R₁—COOH as it forms, to form said polymeric composition.
 18. The method of claim 17, wherein POLYMER2 has the structure

wherein R₂ is selected from the group consisting of hydrogen, methyl, and mixtures thereof, and R₃ is selected from the group consisting of hydrogen, methyl, ethenyl, isopropenyl, carbomethoxy, phenyl, and mixtures thereof.
 19. The method of claim 18, wherein n is between about 50 to about 10,000, m is adjusted such that m/(n+m) is between about 0.0001 to about 0.20, and p is between about 60 to about
 1250. 20. The method of claim 17, wherein POLYMER2 has the structure

wherein R₄ is selected from the group consisting of hydrogen, methyl, and mixtures thereof.
 21. The method of claim 20, wherein n is between about 50 to about 10,000, m is adjusted such that m/(n+m) is between about 0.0001 to about 0.20, 1 is between about 60 to about
 1250. 22. The method of claim 17, wherein POLYMER2 has the structure

wherein Z is selected from the group consisting of O, NH, and mixtures thereof, and R₅ is selected from the group consisting of methyl, ethyl, propyl, and butyl.
 23. The method of claim 22, wherein n is between about 50 to about 10,000, m is adjusted such that m/(n+m) is between about 0.0001 to about 0.20, q is between 4 to about 12, r is between 4 to about 12, s is between about 25 to about
 450. 